Letter to the Editor: Kidney disease

2026-06-11T15:33:33+00:00June 10th, 2026|Categories: Increase Quality of Care, Innovation, Patient Ambassadors, Patient Stories in the News|

I was not looking for kidney disease when it found me. It surfaced during a routine pre-op workup for a completely unrelated procedure. After advocating for myself and pushing for a follow-up, I was diagnosed with chronic kidney disease in 2021. I am not on dialysis yet, but I know it’s not a question of if but when. That reality drives me to advocate. I have friends in the dialysis community living this right now, and I watch them navigate a system that too often fails to keep pace with the treatments that could help them. Innovations in kidney care, [...]

Letter to the editor: Act would restore safeguard for patients

2026-06-11T14:07:39+00:00June 10th, 2026|Categories: Medigap Coverage, Patient Ambassadors, Patient Stories in the News, Private Insurance Coverage, Promote Financial Security|

I have been on hemodialysis for four years. My grandmother was also on dialysis. I started just a year or two after she did. So when I say kidney disease runs in my family, I mean it in the most personal way possible. Dialysis is exhausting. You sit for four to five hours at a time, sometimes dealing with staff who aren't always sensitive to what patients are going through. I am also managing more than just kidney failure. I am a below-the-knee amputee facing a second amputation, and that exhaustion becomes almost unbearable. I started on employer-sponsored private insurance [...]

Kidney disease help

2026-06-09T15:27:45+00:00June 7th, 2026|Categories: Increase Quality of Care, Innovation, Patient Ambassadors, Patient Stories in the News|

In 2020, COVID-19 caused my kidneys to fail. I spent five months in the hospital, four of them on a ventilator, and my wife was called and told to consider pulling the plug and letting me go. I survived, spent two years on peritoneal dialysis, and eventually received a lifesaving kidney transplant in 2023. Living through kidney failure opened my eyes to the fact that too many people don't know what help and resources are available to them, and that's because no one tells them. That has to change, and so does the way we support patients while they're on [...]

Kidney disease is devastating. Congress can help ease journey

2026-06-08T15:52:35+00:00June 5th, 2026|Categories: Medigap Coverage, Patient Ambassadors, Patient Stories in the News, Private Insurance Coverage, Promote Financial Security|

I never knew I was sick. I went to the doctor’s office for a routine procedure, and the lab results sent me straight to the hospital. That was how I learned my kidneys were failing. There was no warning and no symptoms. I was working at AT&T at the time and had private insurance that carried me through. I received a kidney transplant. I was fortunate. My wife worked, and I had faith, family and friends. Not everyone has these luxuries. Now, because of a recent Supreme Court ruling, private insurers can push newly diagnosed dialysis patients off their coverage [...]

Throw kidney disease patients a lifeline

2026-06-02T20:08:18+00:00June 2nd, 2026|Categories: Increase Quality of Care, Innovation, Patient Ambassadors, Patient Stories in the News|

I learned I had polycystic kidney disease just before my wedding. What followed was 13 years of dialysis, the loss of my husband before he could donate his perfectly matched kidney, and years of fighting through grief, illness and uncertainty. Kidney disease affects entire families. In my case, because polycystic kidney disease is genetic, multiple relatives have faced dialysis. That’s why I became an advocate, a social worker and an educator. I’ve spent years writing books and hosting “The Lisa Baxter Show” to help patients understand how to care for themselves and navigate treatment. Patients need more than dialysis. They [...]

Letter: Urging support for Dialysis Patients Act

2026-06-02T20:17:43+00:00June 1st, 2026|Categories: Medigap Coverage, Patient Ambassadors, Patient Stories in the News, Private Insurance Coverage, Promote Financial Security|

To The REVIEW: When I lost my second kidney in my 50s, I was suddenly thrown into a world of dialysis, medical bills and fear. I was self-employed and carried my own insurance, but as my health declined, I became too sick to work. Dialysis is exhausting enough on its own. No patients should also have to spend months or years fighting to keep health coverage and stay financially afloat. Yet, that was my reality. It took two and a half years of fighting before I was finally approved for disability benefits. During that time, medical bills piled up, and [...]

Letter: Protecting dialysis patients

2026-05-28T17:50:56+00:00May 25th, 2026|Categories: Medigap Coverage, Patient Ambassadors, Patient Stories in the News, Private Insurance Coverage, Promote Financial Security|

My father, Earl, treated dialysis like going to work. Diagnosed with diabetes and high blood pressure, he went on dialysis in 2014 and never let it slow him down. He lost weight, got healthier, and even won a Halloween costume contest that fall (my sister dressed him up as a wizard). He was in his 70s and furious about it. That photo is one of our family’s most treasured memories. Through his dialysis journey, I watched my dad find a new community and family at his clinic. I also saw firsthand how vulnerable that lifeline can be and how much [...]

Letter: Restore Protections for Dialysis Patients

2026-05-20T19:03:25+00:00May 19th, 2026|Categories: Medigap Coverage, Patient Ambassadors, Patient Stories in the News, Private Insurance Coverage, Promote Financial Security|

When I was diagnosed with end-stage renal disease in 2017, I was working for a major U.S. airline carrier with strong health insurance coverage. During COVID, as a flight attendant and flight service duty manager with 30 years of experience, I accepted an early-out retirement package. Dialysis had made it increasingly difficult to continue working, and my doctor advised it, given my high risk. As part of that package, I kept active employee-rate health coverage for 36 months. This stability was invaluable and allowed me to delay enrolling in Medicare until the month of my transplant. No dialysis patient should [...]

DPC Gets The Word Out at Detroit Zoo Event

2026-05-28T14:03:58+00:00May 19th, 2026|Categories: Article, Board Members, Get Involved, Medigap Coverage, Patient Ambassadors, State Advocacy, Uncategorized|

On May 17, DPC participated in the National Kidney Foundation Michigan Kidney Walk at the Detroit Zoo. DPC has been working to advance legislation in the state that would expand Medigap access to dialysis patients under 65 years of age. DPC Board President Quiana Bishop and Policy Committee Chair Alethea Walls – both Michigan residents -- recognized this as a great opportunity to get the word out about DPC and recruit additional advocates in support of our advocacy efforts, as NKF Michigan estimated more than 3,000 registered walkers for the event. Michigan Patient Ambassador Gwendolyn Martinez and DPC Eastern Region [...]

Support kidney protection act

2026-05-19T19:07:03+00:00May 18th, 2026|Categories: Increase Quality of Care, Innovation, Patient Ambassadors, Patient Stories in the News|

I was born with kidney failure. I started dialysis at 14, received a transplant at 16, and after 13 years, I’m back on dialysis again. Living with kidney disease my entire life has taught me one thing: access to the right treatment at the right time makes all the difference. Yet too many dialysis patients, especially young people, face constant barriers to innovative therapies. Whether it’s treatments for anemia, infection prevention, or medications to reduce phosphorus, insurance systems fail to keep up with medical advancements. When that happens, patients pay the price with their health. As a patient and someone [...]

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